Literature DB >> 9134025

Use of cryopreserved lymphocytes for assessment of the immunological effects of interferon therapy in renal cell carcinoma patients.

V Sobota1, J Bubeník, M Indrová, V Vlk, J Jakoubková.   

Abstract

Experiments were designed to assess whether cryopreserved PBL could be used to monitor the immunological effects of IFN-alpha therapy in renal cell carcinoma (RCC) patients. It was found that programmed freezing and thawing of peripheral blood lymphocytes (PBL) from normal blood donors did not substantially change lymphocyte subset proportions and that cryopreserved PBL were able to proliferate in response to IL-2. It was also possible to activate the cytolytic activity of frozen PBL, and the frozen leukocytes did not lose their ability to secrete IFN-gamma after PHA activation. We have used these findings to investigate the immunological effects of IFN-alpha therapy in RCC patients. Cryopreservation of PBL samples collected from various patients over a period of 9-14 months enabled us to compare the in vitro reactivity of PBL from individual RCC patients repeatedly and under standard conditions. It was found that IL-2 induced proliferative responses of PBL from IFN-alpha non-responders, collected prior to IFN-alpha therapy, were significantly decreased as compared to those from normal blood donors. The proliferative responses of PBL from IFN-alpha responders, collected prior to IFN-alpha therapy, did not substantially differ from normal controls. Culture of PBL from IFN-alpha responders for 3 days in IFN-alpha-containing medium increased their lytic activity towards RCC targets, whereas no such increase was observed with non-RCC targets or using PBL from IFN-alpha non-responders or PBL from normal-blood donors. Enzyme-linked immunospot (ELISPOT) assays performed with cryopreserved lymphocytes from IFN-alpha non-responding RCC patients, collected prior to IFN-alpha therapy, revealed a substantially decreased ability to secrete IFN-gamma, as compared to IFN-gamma secretion of PBL from IFN-alpha responders or normal blood donors.

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Year:  1997        PMID: 9134025     DOI: 10.1016/s0022-1759(97)00020-3

Source DB:  PubMed          Journal:  J Immunol Methods        ISSN: 0022-1759            Impact factor:   2.303


  7 in total

1.  Preservation of lymphocyte immunophenotype and proliferative responses in cryopreserved peripheral blood mononuclear cells from human immunodeficiency virus type 1-infected donors: implications for multicenter clinical trials. The ACTG Immunology Advanced Technology Laboratories.

Authors:  K A Reimann; M Chernoff; C L Wilkening; C E Nickerson; A L Landay
Journal:  Clin Diagn Lab Immunol       Date:  2000-05

2.  Development and validation of a gamma interferon ELISPOT assay for quantitation of cellular immune responses to varicella-zoster virus.

Authors:  J G Smith; X Liu; R M Kaufhold; J Clair; M J Caulfield
Journal:  Clin Diagn Lab Immunol       Date:  2001-09

3.  Standardized Serum-Free Cryomedia Maintain Peripheral Blood Mononuclear Cell Viability, Recovery, and Antigen-Specific T-Cell Response Compared to Fetal Calf Serum-Based Medium.

Authors:  Anja Germann; Julia C Schulz; Beatrice Kemp-Kamke; Heiko Zimmermann; Hagen von Briesen
Journal:  Biopreserv Biobank       Date:  2011-09       Impact factor: 2.300

4.  Use of transcriptional signatures induced in lymphoid and myeloid cell lines as an inflammatory biomarker in Type 1 diabetes.

Authors:  Shuang Jia; Mary Kaldunski; Parthav Jailwala; Rhonda Geoffrey; Joanna Kramer; Xujing Wang; Martin J Hessner
Journal:  Physiol Genomics       Date:  2011-03-15       Impact factor: 3.107

5.  Loss of T cell responses following long-term cryopreservation.

Authors:  Rachel E Owen; Elizabeth Sinclair; Brinda Emu; John W Heitman; Dale F Hirschkorn; C Lorrie Epling; Qi Xuan Tan; Brian Custer; Jeffery M Harris; Mark A Jacobson; Joseph M McCune; Jeffery N Martin; Frederick M Hecht; Steven G Deeks; Philip J Norris
Journal:  J Immunol Methods       Date:  2007-08-08       Impact factor: 2.303

6.  Impact of cryopreservation on tetramer, cytokine flow cytometry, and ELISPOT.

Authors:  Holden T Maecker; James Moon; Sonny Bhatia; Smita A Ghanekar; Vernon C Maino; Janice K Payne; Kristine Kuus-Reichel; Jennie C Chang; Amanda Summers; Timothy M Clay; Michael A Morse; H Kim Lyerly; Corazon DeLaRosa; Donna P Ankerst; Mary L Disis
Journal:  BMC Immunol       Date:  2005-07-18       Impact factor: 3.615

7.  Standardization and performance evaluation of mononuclear cell cytokine secretion assays in a multicenter study.

Authors:  Wayne G Shreffler; Cynthia M Visness; Melissa Burger; William W Cruikshank; Howard M Lederman; Maite de la Morena; Kristine Grindle; Agustin Calatroni; Hugh A Sampson; James E Gern
Journal:  BMC Immunol       Date:  2006-12-12       Impact factor: 3.615

  7 in total

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